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rs782252317

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs782252317(A;A)
Make rs782252317(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77142763
GeneMYO7A
is asnp
is mentioned by
dbSNPrs782252317
ebirs782252317
HLIrs782252317
Exacrs782252317
Varsomers782252317
Maprs782252317
PheGenIrs782252317
hapmaprs782252317
1000 genomesrs782252317
hgdprs782252317
ensemblrs782252317
gopubmedrs782252317
geneviewrs782252317
scholarrs782252317
googlers782252317
pharmgkbrs782252317
gwascentralrs782252317
openSNPrs782252317
23andMers782252317
23andMe allrs782252317
SNP Nexus

SNPshotrs782252317
SNPdbers782252317
MSV3drs782252317
GWAS Ctlgrs782252317
Max Magnitude0
ClinVar
Risk rs782252317(A;A)
Alt rs782252317(A;A)
Reference rs782252317(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76853809G>A
CLNSRC
CLNACC RCV000154329.1,